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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará la selección de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por International Parkinson & Movement Disorder Society.

Corea y enfermedad de Huntington

450 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Putting the Brakes on Huntington Disease in a Mouse Experimental Model.

Kim JC, Mirkin SM.

PLoS Genet. 2015 Aug 6;11(8):e1005409. doi: 10.1371/journal.pgen.1005409. No abstract available.

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Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study.

Røthing M, Malterud K, Frich JC.

Health Soc Care Community. 2015 Sep;23(5):569-76. doi: 10.1111/hsc.12174.

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PUBMED

HTT/Huntingtin in selective autophagy and Huntington disease: A foe or a friend within?

Rui YN, Xu Z, Patel B, Cuervo AM, Zhang S.

Autophagy. 2015;11(5):858-60. doi: 10.1080/15548627.2015.1039219. No abstract available.

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PUBMED

Deep brain stimulation in Huntington's disease: assessment of potential targets.

Sharma M, Deogaonkar M.

J Clin Neurosci. 2015 May;22(5):812-7. doi: 10.1016/j.jocn.2014.11.008. Review.

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Transcriptional dysregulation in Huntington's disease: The role of histone deacetylases.

Sharma S, Taliyan R.

Pharmacol Res. 2015 Oct;100:157-69. doi: 10.1016/j.phrs.2015.08.002. Review.

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PUBMED

Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains.

Bai G, Cheung I, Shulha HP, Coelho JE, Li P, Dong X, Jakovcevski M, Wang Y, Grigorenko A, Jiang Y, Hoss A, Patel K, Zheng M, Rogaev E, Myers RH, Weng Z, Akbarian S, Chen JF.

Hum Mol Genet. 2015 Mar 1;24(5):1441-56. doi: 10.1093/hmg/ddu561.

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PUBMED

High Protein Diet and Huntington's Disease.

Chen CM, Lin YS, Wu YR, Chen P, Tsai FJ, Yang CL, Tsao YT, Chang W, Hsieh IS, Chern Y, Soong BW.

PLoS One. 2015 May 19;10(5):e0127654. doi: 10.1371/journal.pone.0127654.

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PUBMED

Neonatal iron supplementation potentiates oxidative stress, energetic dysfunction and neurodegeneration in the R6/2 mouse model of Huntington's disease.

Berggren KL, Chen J, Fox J, Miller J, Dodds L, Dugas B, Vargas L, Lothian A, McAllum E, Volitakis I, Roberts B, Bush AI, Fox JH.

Redox Biol. 2015;4:363-74. doi: 10.1016/j.redox.2015.02.002.

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PUBMED

Language Impairment in Adolescents With Sydenham Chorea.

Harsányi E, Moreira J, Kummer A, Meira ZM, Cardoso F, Teixeira AL.

Pediatr Neurol. 2015 Nov;53(5):412-6. doi: 10.1016/j.pediatrneurol.2015.06.022.

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PUBMED

Intra-individual Variability in Prodromal Huntington Disease and Its Relationship to Genetic Burden.

Musso M, Westervelt HJ, Long JD, Morgan E, Woods SP, Smith MM, Lu W, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group..

J Int Neuropsychol Soc. 2015 Jan;21(1):8-21. doi: 10.1017/S1355617714001076.

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PUBMED

Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice.

Kurosawa M, Matsumoto G, Kino Y, Okuno M, Kurosawa-Yamada M, Washizu C, Taniguchi H, Nakaso K, Yanagawa T, Warabi E, Shimogori T, Sakurai T, Hattori N, Nukina N.

Hum Mol Genet. 2015 Feb 15;24(4):1092-105. doi: 10.1093/hmg/ddu522.

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PUBMED

Counterfactual Thinking Deficit in Huntington's Disease.

Solca F, Poletti B, Zago S, Crespi C, Sassone F, Lafronza A, Maraschi AM, Sassone J, Silani V, Ciammola A.

PLoS One. 2015 Jun 12;10(6):e0126773. doi: 10.1371/journal.pone.0126773.

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PUBMED

Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice.

Achour M, Le Gras S, Keime C, Parmentier F, Lejeune FX, Boutillier AL, Néri C, Davidson I, Merienne K.

Hum Mol Genet. 2015 Jun 15;24(12):3481-96. doi: 10.1093/hmg/ddv099.

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PUBMED

Neuroprotective properties of cannabigerol in Huntington's disease: studies in R6/2 mice and 3-nitropropionate-lesioned mice.

Valdeolivas S, Navarrete C, Cantarero I, Bellido ML, Muñoz E, Sagredo O.

Neurotherapeutics. 2015 Jan;12(1):185-99. doi: 10.1007/s13311-014-0304-z.

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PUBMED

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.

Krause A, Mitchell C, Essop F, Tager S, Temlett J, Stevanin G, Ross C, Rudnicki D, Margolis R.

Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):573-85. doi: 10.1002/ajmg.b.32332.

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